1 / 25

Horng H Chen MD on behalf of the NHLBI Heart Failure Clinical Research Network

R enal O ptimization S trategies E valuation in Acute Heart Failure (ROSE AHF): A Randomized Clinical Trial. Horng H Chen MD on behalf of the NHLBI Heart Failure Clinical Research Network. Background AHF + Renal Dysfunction.

james-rush
Download Presentation

Horng H Chen MD on behalf of the NHLBI Heart Failure Clinical Research Network

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Renal Optimization StrategiesEvaluation in Acute Heart Failure (ROSE AHF):A Randomized Clinical Trial Horng H Chen MD on behalf of the NHLBI Heart Failure Clinical Research Network

  2. BackgroundAHF + Renal Dysfunction • Patients with acute heart failure (AHF) and renal dysfunction are at risk for inadequate decongestion and worsening renal function – factors associated with adverse clinical outcomes.

  3. BackgroundLow dose dopamine • Low or “renal” dose dopamine may selectively activate dopamine receptors and promote renal vasodilatation. • Previous small studies suggest that low dose dopamine (2-5 g/kg/min) may enhance decongestion and preserve renal function during diuretic therapy in AHF.

  4. BackgroundLow dose nesiritide • Nesiritide at recommended dose (2 g/kg bolus + 0.01 g/kg/min infusion) lowers blood pressure and does not favorably impact renal function or clinical outcomes. • Previous small studies suggest that low dose nesiritide (0.005 g/kg/min without bolus) may have renal specific actions which enhance decongestion and preserve renal function during diuretic therapy in AHF.

  5. HypothesesNovel study design In patients with AHF and renal dysfunction: I. As compared to placebo, the addition of low dose dopamine (2 g/kg/min) to diuretic therapy will enhance decongestion and preserve renal function II. As compared to placebo, the addition of low dose nesiritide (0.005 g/kg/min without bolus) to diuretic therapy will enhance decongestion and preserve renal function.

  6. Study Population • Diagnosis of AHF: • ≥1 symptom (dyspnea, orthopnea, edema) • ≥ 1 sign (rales, edema, ascites, CXR) • Enrolled within 24 hours of hospital admission • Estimated GFR of 15 - 60 mL/min/1.73m2 • Modification of diet in renal disease equation

  7. Study Design Standardized Diuretic Dosing For 1st 24 hours 2.5 x Outpt Furosemide Equivalent in Divided (BID) IV Doses

  8. Co-Primary Endpoints • Decongestion Endpoint: Cumulative urinary volume from randomization through 72 hours • Renal Function Endpoint : Change in serum cystatin-C from randomization to 72 hours

  9. Secondary Endpoints Decongestion endpoints • Change in weight: randomization to 72 hrs, • Change in NT-proBNP: randomization to 72 hrs Renal function endpoints • Change in creatinine: randomization to 72 hrs, • Cardio-renal syndrome (↑Cr > 0.3 mg/dL) Symptom relief endpoints • Dyspnea VAS; AUC over 72 hrs Clinical endpoints • Drug tolerance • Adverse events

  10. Statistical Methods • > 85% power to detect effect (p<0.025) of • 72 urine volume of > 1400 ml • Change in cystatin C of > 0.3 mg/L • Treatment comparisons by “intention to treat” • Multiple imputation for missing data. • Conservative framework for subgroup interaction testing (interaction p-value <0.01)

  11. Baseline Characteristics Median or % shown; No significant between group differences

  12. Baseline Characteristics Median or % shown; No significant between group differences

  13. ResultsDopamine Strategy

  14. Low Dose Dopamine: Co-primary End-points 72 Hour Urine Volume Change in Cystatin-C

  15. Low Dose DopamineSub-group Analysis

  16. Low Dose DopamineSecondary Endpoints • No significant treatment effect on secondary endpoints reflective of: • Decongestion • Renal function • Symptom relief

  17. Low Dose Dopamine Clinical Outcomes 60 Day Death/ Unscheduled visit/ HF Readmission 180 Day Mortality

  18. ResultsNesiritide Strategy

  19. Low Dose Nesiritide Co-primary End-points 72 Hour Urine Volume Change in Cystatin-C

  20. Low Dose Nesiritide Sub-group Analysis

  21. Low Dose NesiritideSecondary Endpoints • No significant treatment effect on secondary endpoints reflective of: • Decongestion • Renal function • Symptom relief

  22. Low Dose Nesiritide Clinical Outcomes 60 Day Death/ Unscheduled visit/ HF Readmission 180 Day Mortality

  23. Conclusions • In patients with AHF and underlying renal dysfunction, when added to standardized diuretic dosing, neither low dose dopamine, nor low dose nesiritide, enhanced decongestion or improved renal function. • Future investigations of these or other acute heart failure therapies may need to assess the potential for differential responses in heart failure with preserved versus reduced ejection fraction.

  24. Minnesota Heart Failure Consortium Montreal Heart Institute University of Vermont/Tufts University Harvard University Mayo Clinic U. Pennsylvania University of Utah Cleveland Thomas Jefferson University NHLBI Washington University Duke University DCRI Emory University Morehouse School of Medicine Baylor College of Medicine

  25. HH Chen and coauthors Low-Dose Dopamine or Low-Dose Nesiritide in Acute Heart Failure With Renal Dysfunction: The ROSE Acute Heart Failure Randomized Trial Published online November 18, 2013

More Related